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Diseases
Genes (1489)
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TTPA
Visual Impairment
Familial Isolated Vitamin E Deficiency
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
ABCC2
Dubin-Johnson Syndrome
ABCC9
Cantú Syndrome
ADGRG1
Bilateral Frontoparietal Polymicrogyria
PQBP1
Renpenning's Syndrome
NRAS
Acute Promyelocytic Leukemia
Melanocytic Nevus Syndrome, Congenital
NPM1
Classic Mycosis Fungoides
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
KCNJ8
Cantú Syndrome
NUMA1
Acute Promyelocytic Leukemia
PLVAP
Diarrhea 7, Protein-Losing Enteropathy Type
CSF2RA
Hereditary Pulmonary Alveolar Proteinosis
LIPA
Acid Lipase Disease
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia
STAT5B
Acute Promyelocytic Leukemia